European Journal of Paediatric Neurology

Papers
(The TQCC of European Journal of Paediatric Neurology is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-02-01 to 2025-02-01.)
ArticleCitations
Diagnostic accuracy is required when analysing cohorts with mitochondrial disorders62
Early motor, cognitive, language, behavioural and social emotional development in infants and young boys with Duchenne Muscular Dystrophy- A systematic review37
Dystonia in children with acquired brain injury30
Associations between muscle morphology and spasticity in children with spastic cerebral palsy29
Quality of life and neurological disability in children and young people with ataxia telangiectasia29
Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiency26
Editorial Board26
Autonomic risks in Alternating Hemiplegia of Childhood25
Neurophysiological recordings improve the accuracy of the evaluation of the outcome in perinatal hypoxic ischemic encephalopathy24
Applicability of quantitative oculomotor and SARA assessment in children22
Urgent unmet need for pharmaceutical grade vitamin therapy in pyridoxine dependent epilepsies19
Deep brain stimulation for phantom limb pain19
Jeavons syndrome featured with visual sensitivity existing as occipital cortex originating focal-to-generalized continuum epilepsy19
46th Annual Conference of the German Neuropaediatric Society (GNP) and 17th GNP Training Course Academy19
Are atypical knee jerk responses prognostic for cerebral palsy in high-risk infants and children?17
Vaccination in pediatric acquired inflammatory immune-mediated neuromuscular disorders16
Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype16
Effects of thalamic and basal ganglia deep brain stimulation on language-related functions – Conceptual and clinical considerations16
Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency15
Association between vitamin B12 deficiency and risk of Paediatric narcolepsy: Evidence from cross-sectional study and Mendelian randomization analysis14
Ocrelizumab in pediatric patients with MS: Efficacy, tolerability, and safety14
Adolescents with Rett syndrome at critical care pathway junctures: Examining clinicians’ decision to initiate invasive long-term ventilation14
‘Focal Seizures in Dystonic Cerebral Palsy (DCP): Rare or common or both?14
Be aware of childhood stroke: Proceedings from EPNS Webinar14
Anticoagulation for pediatric head-injury-related cerebral sinovenous thrombosis. A call for trial-derived evidence to standardize anticoagulant management13
Editorial Commentary on “Sonographic evaluations of the skeletal muscles in patients with Pompe disease” by Y.H. Chiu et al.13
Analysis of the relation between cerebrospinal fluid antibody titers and clinical characteristics in pediatric patients with anti-N-methyl-D-aspartate receptor encephalitis13
The pathogenetic basis for a disease continuum in early- and late-onset ataxia-dystonia supports a unified genetic diagnostic approach13
Epidemiology of traumatic brain injury in children 15 years and younger in South-Eastern Norway in 2015–16. Implications for prevention and follow-up needs12
Motor imagery ability of children with duchenne muscular dystrophy: Reliability and validity of kinesthetic and Visual Imagery Questionnaire-10, and its association with cognitive status12
School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort study12
Validation of the Internet Addiction Test for Adolescents (IAT-A) in the Georgian language12
Characterization of sedation and anesthesia complications in patients with alternating hemiplegia of childhood12
Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay11
Endovascular and thrombolytic treatment eligibility in childhood arterial ischemic stroke10
Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatment10
Characterising the typical range of influenza-associated neurological symptoms in children10
Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review10
Cognitive and neurological outcome of patients in the Dutch pyridoxine-dependent epilepsy (PDE-ALDH7A1) cohort, a cross-sectional study10
Repetitive neuromuscular magnetic stimulation in children with headache10
Mental health and behaviour in children with dystonia: Anxiety, challenging behaviour and the relationship to pain and self-esteem9
Genetic causes underlying grey matter heterotopia9
Endocrine and metabolic aspects of narcolepsy type 1 in children9
Visual outcome measures in pediatric myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD)9
Functional brain maturation and sleep organisation in neonates with congenital heart disease9
Is ketogenic diet a ‘precision medicine’? Recent developments and future challenges9
Abnormal frontal gyrification pattern and uncinate development in patients with KBG syndrome caused by ANKRD11 aberrations9
Predicting respiratory failure and outcome in pediatric Guillain-Barré syndrome9
2024 update: European consensus statement on gene therapy for spinal muscular atrophy9
Vaccination and childhood epilepsies9
Application of the Scale for Assessment and Rating of Ataxia in toddlers8
Autoimmune encephalitis in Israeli children – A retrospective nationwide study8
Participation after childhood stroke: Is there a relationship with lesion size, motor function and manual ability?8
Vitamin deficiencies in children: Lessons from clinical and neuroimaging findings8
Neurologic complications of thiamine (B1) deficiency following bariatric surgery in adolescents8
A novel family illustrating the mild phenotypic spectrum of TUBB2B variants8
Acute necrotizing encephalopathy infected with the SARS-CoV-2 in children: Case series and literature review of clinical outcomes with the use of Tocilizumab8
Epidemiology of paediatric moderate and severe traumatic brain injury in the Netherlands8
Outcomes for patients in the RESTORE registry with spinal muscular atrophy and four or more SMN2 gene copies treated with onasemnogene abeparvovec7
A life course perspective on mental disorders and psychopharmacologic drug use among persons living with cerebral palsy7
Fulfilling the needs of caregivers in delivering health services to children with developmental and epileptic encephalopathies7
Is CSF hypocretin level useful for differentiating narcolepsy type 1 and 2?7
Report from the child neurology education and training workshop at the International Child Neurology Congress 2024: Expert's addressing the training gap7
Ketogenic diet registry for epilepsy: A cross-sectional feasibility study7
Validation of the 2023 international diagnostic criteria for MOGAD in a pediatric cohort7
Somatosensory profile in individuals with duchenne muscular dystrophy: A quantitative sensory testing (QST) study7
Predictive value of brain MRI for neurodevelopmental outcome in infants with severe unconjugated hyperbilirubinemia: A systematic review7
Corrigendum to “Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes” [Europ. J. Paediatr. Neurol. 41 (2022) 8–18 doi.org/10.1016/7
Epilepsy with myoclonic-atonic seizures, also known as Doose syndrome: Modification of the diagnostic criteria7
What you see is what you get? Eye gaze as a window to vocabulary in Rett Syndrome6
The use of intrathecal baclofen for management of spasticity in hereditary spastic paraparesis: A case series6
Therapeutic hypothermia is associated with changes in prognostic value of general movements6
Editorial Board6
Identification of novel pathogenic variants in the GCDH gene and assessment of neurodevelopmental outcomes in 24 children with glutaric aciduria type 16
Trauma, coping, and adjustment when parenting a child with Dravet syndrome6
The burden of neurological disorders in the pediatric emergency setting: Insight for planning the neurological care6
CCL2/MCP-1, interleukin-8, and fractalkine/CXC3CL1: Potential biomarkers of epileptogenesis and pharmacoresistance in childhood epilepsy6
Frequency and clinical relevance of MOG-antibodies in CSF in pediatric patients with MOG antibody-associated diseases6
Incidence, and factors associated with moderate/severe pediatric traumatic brain injury in children aged 5–15 years in western, Mexico6
Autoantibody status, neuroradiological and clinical findings in children with acute cerebellitis6
Bradykinesia assessment in children with cerebral palsy and periventricular leukomalacia6
Strength measurements in patients with Dravet Syndrome6
Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life6
Editorial Board6
Melatonin for neuroprotection in neonatal encephalopathy: A systematic review & meta-analysis of clinical trials6
Neurological and psychiatric phenotype of a multicenter cohort of patients with SETD5-related neurodevelopmental disorder6
May intraoperative detection of stereotactically inserted intracerebral electrodes increase precision of resective epilepsy surgery?6
Neurological presentations and cognitive outcome in Sturge-Weber syndrome6
Quality of life in ataxia-telangiectasia6
Long-term monitoring of children with Pseudo Tumor Cerebri Syndrome by transbulbar sonography6
Visual processing difficulties in children with NF1. A common but not widely recognized underlying cause of reading difficulties6
Difficulty of administration of nusinersen in complex-column spinal muscular atrophy: New alternative technique by means of cervical intrathecal access through an Ommaya reservoir6
Neurologic manifestations in children with COVID-196
Safety and feasibility of transcranial direct current stimulation stratified by corticospinal organization in children with hemiparesis6
Specific characteristics and current diagnostic and treatment modalities performance of super refractory status epilepticus in children: A comparative study5
Characterizing, classifying, and collecting spells in paroxysmal disorders – A need as targeted therapies approach for childhood neurological disorders5
Translational research for the development of treatment of patients with neurogenetic diseases: An important step for Angelman syndrome5
Basal ganglia: From the bench to the bed5
Trajectories of motor function in children with Duchenne muscular dystrophy: A longitudinal study on a Colombian population5
The added value of multimodal neurophysiological tools in the prognostic assessment of perinatal hypoxic-ischemic encephalopathy5
Bimanual performance in children with unilateral perinatal arterial ischaemic stroke or periventricular haemorrhagic infarction5
The importance of dystonia in cerebral palsy5
Advances in genetics: The start of a new stage for management of focal cortical malformations5
Neurobiological developmental disorders – The challenging assessment of the needs of children and adolescents5
Dysmature patterns of newborn EEG recordings: Biological markers of transitory brain dysfunction or brain injury5
Editorial: Motor Function Measure in Duchenne Muscular Dystrophy5
PNS or not PNS, a dilemma of the post-genomic era in neurogenic developmental disorders5
Yield of exome sequencing in patients with developmental and epileptic encephalopathies and inconclusive targeted gene panel5
Comparison of clinical characteristics between cluster and isolated seizures associated with benign convulsions with mild gastroenteritis5
Editorial Board5
Knowledge, awareness, and attitudes towards epilepsy among elementary schoolteachers in the Kingdom of Bahrain5
Optimizing neonatal outcomes with melatonin - Huge promise but slow progress4
Language outcomes in children who underwent surgery for the removal of a posterior fossa tumor: A systematic review4
“Fidgety-like movements” in extremely preterm infants - A new entity of spontaneous movements4
Delineation of the phenotype of MED17-related disease in Caucasus-Jewish families4
Distinct attentional and executive profiles in neurofibromatosis type 1: Is there difference with primary attention deficit-hyperactivity disorder?4
The spectrum of acute leukoencephalopathy with restricted diffusion (ALERD): A case series and review of literature4
Deep brain stimulation-induced neuroprotection: A critical appraisal4
Neurocognitive profile of a cohort of SMA type 1 pediatric patients and emotional aspects, resilience and coping strategies of their caregivers4
Starting a DBS service for children: It’s not the latitude but the attitude - Establishment of the paediatric DBS centre in Northern Finland4
Relationship between 4-month functional brain network topology and 24-month neurodevelopmental outcome in children with congenital heart disease4
Dystonia assessment in children with cerebral palsy and periventricular leukomalacia4
Gaboxadol in angelman syndrome: A double-blind, parallel-group, randomized placebo-controlled phase 3 study4
Development of muscle tone impairments in high-risk infants: Associations with cerebral palsy and cystic periventricular leukomalacia4
Cognitive function, behaviour and quality of life in children with myotonic dystrophy type 1 in South - Eastern Norway4
Commentary on “Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study”4
Early MRI diagnosis of Sturge Weber Syndrome type 1 in infants4
Identification of PMD subgroups using a myelination score for PMD4
Post traumatic cerebral sinovenous thrombosis in children: A retrospective and multicenter study4
Clinical features and outcomes of opsoclonus myoclonus ataxia syndrome4
Clinical and radiological findings of posterior reversible encephalopathy syndrome in children: About 16 children hospitalized in the pediatric department of a Tunisian tertiary care hospital4
Paediatric neurocysticercosis in high income countries4
Moving across disorders: A cross-sectional study of cognition in early onset ataxia and dystonia4
Pre-surgical evaluation challenges and long-term outcome in children operated on for Low Grade Epilepsy Associated brain Tumors4
A patient centered view of randomized control trial data: An example with fenfluramine for Dravet syndrome4
Myotonic dystrophy type 1 (Steinert disease): 29 years of experience at a tertiary pediatric hospital4
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study4
The importance of long term follow-up in children with acquired demyelinating syndromes4
Exploring demographic, medical, and developmental determinants of adaptive behaviour in children with hemiplegic cerebral palsy4
The epileptology of Wiedemann-Steiner syndrome: Electroclinical findings in five patients with KMT2A pathogenic variants4
Room to improve: The diagnostic journey of Spinal Muscular Atrophy4
EPITRANS. Quality assessment of the epilepsy transition process4
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